Deubiquitinating enzymes: Promising targets for drug resistance.

Apoptosis DNA repair Deubiquitinating enzymes Drug resistance Signaling pathways Therapeutic targets Transcription factors

Journal

Drug discovery today
ISSN: 1878-5832
Titre abrégé: Drug Discov Today
Pays: England
ID NLM: 9604391

Informations de publication

Date de publication:
09 2022
Historique:
received: 03 02 2022
revised: 05 05 2022
accepted: 22 06 2022
pubmed: 28 6 2022
medline: 31 8 2022
entrez: 27 6 2022
Statut: ppublish

Résumé

Drug resistance to chemotherapy and molecularly targeted therapies is a current challenge in cancer treatments. The underlying mechanisms of resistance to cytotoxic chemotherapeutics and to drugs that target a specific molecule are not understood completely. In recent years, emerging evidence has frequently suggested that the dysregulation of deubiquitinating enzymes (DUBs) plays important roles in the development of drug resistance. We focus on the molecular mechanisms through which DUBs enable cancer cells to escape cell death and survive when exposed to a variety of anti-cancer drugs. Furthermore, this review summarizes the potential application of DUB inhibitors in combination therapies to overcome drug resistance.

Identifiants

pubmed: 35760282
pii: S1359-6446(22)00279-3
doi: 10.1016/j.drudis.2022.06.009
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
Deubiquitinating Enzymes EC 3.4.19.12

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2603-2613

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interests The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Fujing Ge (F)

Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.

Yuekang Li (Y)

Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.

Tao Yuan (T)

Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.

Yulian Wu (Y)

The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.

Qiaojun He (Q)

Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China; The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China; Innovation Institute for Artificial Intelligence in Medicine, Zhejiang University, Hangzhou, China.

Bo Yang (B)

Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China. Electronic address: yang924@zju.edu.cn.

Hong Zhu (H)

Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China; The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China; The Westlake Laboratory of Life Sciences and Biomedicine, Hangzhou, China. Electronic address: hongzhu@zju.edu.cn.

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Classifications MeSH